A.M. Jahangir Alam
Department of Medicine, Mymensingh Medical College, Bangladesh
Publications
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Case Report
Acute Interstitial Nephritis as the First Presenting Feature of Wilson's Disease: A case Report of Diagnostic Dilemma
Author(s): Ashmita Yadav*, Ram Bahadur Nepali and A.M. Jahangir Alam
Introduction: Wilson's disease( also called as hepaticolenticular degeneration) is a rare genetic (autosomal recessive) disorder resulting from mutation in ATP7B gene presenting with features affecting various organs of the body namely( liver, brain, kidney, cornea) due to deposition of excess copper in these organs. It can lead to fatal consequences if not diagnosed and treated in time however prompt diagnosis and treatment can prevent further deterioration of symptoms. Case Presentation: The authors hereby present a case of 11 years old male who presented with symptoms mimicking post streptococcal glomerulonephritis (PSGN) however after a thorough history , clinical examination findings and detailed investigations he was diagnosed as a case of decompensated chronic liver disease (CLD) due to Wilson’s disease with acute interstiti.. Read More»

